Cerebrovascular accident and hyperhomocysteinemia;Cerebrovasculair accident en hyperhomocysteïnemie

Tijdschrift voor Geneeskunde

Volumn 57, Issue 6, 2001, Pages 463-468

  Vanbrabant, P ^a   Van Den Bosch, G ^a   Gheuens, E ^a   Baeck, E ^a   Nuytten, D ^a   Neels, H ^a   Verbraeken, H ^a  

^a NONE   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTATHIONINE BETA SYNTHASE; HOMOCYSTEINE;

ADULT; ANGIOGRAPHY; ARTICLE; CASE REPORT; CEREBROVASCULAR ACCIDENT; CLINICAL EXAMINATION; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC IMAGING; HOMOCYSTINURIA; HOMOZYGOSITY; HUMAN; HYPERHOMOCYSTEINEMIA; LABORATORY DIAGNOSIS; MORTALITY; PATHOGENESIS; RISK FACTOR;

EID: 0035868836     PISSN: 0371683X     EISSN: None     Source Type: Journal    
DOI: 10.2143/tvg.57.6.1001006     Document Type: Article

References (16)

1. Vascular pathology of homocysteinemia: Implications for the pathogenesis of arteriosclerosis
2. Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project
3. Nonfasting plasma total homocysteine level and mortality in middle-aged and elderly men and women in Jerusalem
4. Nonfasting plasma total homocysteine levels and stroke incidence in elderly persons: The Framingham Study
5. Homocysteine and atherothrombosis
6. Hyperhomocysteïnemie: Ontstaan, pathologie en behandeling
7. Homocystinuria due to cystathionine-β-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control
8. Circulating lipid hydroperoxide levels in human hyperhomocysteinemia. Relevance to development of arteriosclerosis
9. Hyperhomocysteïnemie als risicofactor voor atherosclerose en thrombose
10. Lowered antithrombin III activity and other clotting changes in homocystinuria: Effects of a pyridoxine-folate regimen
11. Coalgulation factors and markers of activation of coagulation in homocystinuria (HOCY): A study in two siblings
12. Homocystinuria due to cystathionine-β-synthase deficiency and related disorders
13. The natural history of homocystinuria due to cystathionine-β-synthase deficiency
14. Strategies for the treatment of cystathionine beta-synthase deficiency: The experience of the Willink Biochemical Genetics Unit over the past 30 years
15. Disorders of transsulfuration
16. Reduction of false negative results in screening of newborns for homocystinuria